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Vind je volgende functie in Regulatory Affairs binnen Life Sciences en help conforme markttoegang en regulatoire excellentie te garanderen bij de toonaangevende bedrijven in België.
Our client, a leading organization in the life sciences sector, is seeking a dedicated professional to join their laboratory team. The role involves performing and evaluating complex analytical and microbiological tests within a strictly regulated quality control environment.
Our client, a prominent pharmaceutical organization, is looking for a hands-on Production Engineer to provide first-line technical support. This role ensures the continuity of the production line by troubleshooting process issues and coordinating team activities within a regulated environment.
Our client, a leading organization in the pharmaceutical sector, is seeking a professional to support engineering and construction projects at a GMP-regulated site. This role involves taking ownership of safety aspects during the design and realization phases, ensuring both process and construction safety for diverse project scopes.
Our client, a leading pharmaceutical company, is seeking a motivated professional to join their advanced analytical characterization team. This laboratory-based role involves developing innovative imaging solutions for active pharmaceutical ingredients and complex drug delivery systems.
Our client, a leading pharmaceutical organization, is seeking an Equipment Validation Engineer to ensure the reliable and compliant operation of production systems. The role focuses on managing validation documentation and testing for mechanical equipment within multidisciplinary engineering and production projects.
Of je nu gespecialiseerd bent in regulatory strategie, compliance of etikettering: bij ons vind je kansen in uiteenlopende specialisaties.
Regulatory Strategist – Bepaal en begeleid de regulatory strategie doorheen het volledige ontwikkeltraject.
Regulatory Affairs Expert – Bied ondersteuning bij de voorbereiding, indiening en opvolging van regulatoire dossiers.
Regulatory Affairs Specialist – Zorg voor naleving van de Belgische, Europese en internationale regelgeving voor geneesmiddelen.
Artwork & Labeling Consultant – Beheer het labelingproces en voer artworkcontroles uit volgens de geldende richtlijnen.
Labeling Specialist – Waak over correcte en conforme productinformatie voor verschillende markten.
CMC Regulatory Affairs Consultant – Verzorg de indiening van regulatoire CMC-dossiers (Chemistry, Manufacturing & Controls).
Regulatory Projectcoördinator – Coördineer deadlines, dossiers en communicatie met stakeholders.
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